Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype

Diego Ojeda, Besma Lakhal, Dora Janneth Fonseca, Rim Braham, Hanne Landolsi, Heidi Eliana Mateus, Carlos Martín Restrepo, Hatem Elghezal, Ali Saâd, Paul Laissue

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Medicine & Life Sciences